Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409, USA.
Analyst. 2013 Sep 7;138(17):4892-7. doi: 10.1039/c3an01142a. Epub 2013 Jul 8.
In the present study, early stage apoptosis is explored with high temporal resolution. In addition to monitoring early apoptosis induction in single cells by ultrasensitive confocal fluorescence microscopy (UCFM), the mitochondrial protein release kinetics was explored. The current study shows development and optimization of a novel, rapid apoptosis assay to explore the earliest changes in cells by the intrinsic apoptosis pathway. We show that early apoptotic changes in the mitochondria begin nearly simultaneously with the addition of an apoptosis-inducing drug, such as staurosporine. With a temporal resolution of five minutes, this non-invasive analytical technique can elucidate the earliest apoptotic events in living cells. Moreover, our results show that the mitochondrial inter-membrane proteins are not involved in the extrinsic pathway of Ramos cells mediated by an anti-CD95 antibody. Additional techniques such as light microscopy and flow cytometry were employed to confirm the results obtained by ultrasensitive confocal fluorescence microscopy. The results of this study help to understand the earliest mechanisms of apoptosis induction in cells, enabling new methods of drug testing and dose-response analyses.
在本研究中,我们以高时间分辨率探索早期细胞凋亡。除了通过超高灵敏度共聚焦荧光显微镜(UCFM)监测单个细胞中早期细胞凋亡的诱导外,我们还探索了线粒体蛋白释放动力学。本研究展示了一种新型快速细胞凋亡检测方法的开发和优化,旨在通过内在凋亡途径探索细胞中最早的变化。我们表明,在添加诱导细胞凋亡的药物(如星形孢菌素)时,线粒体中早期凋亡变化几乎同时发生。通过五分钟的时间分辨率,这种非侵入性分析技术可以阐明活细胞中最早的细胞凋亡事件。此外,我们的结果表明,线粒体膜间蛋白不参与由抗 CD95 抗体介导的 Ramos 细胞的外在途径。还使用了其他技术,如光学显微镜和流式细胞术,以确认超高灵敏度共聚焦荧光显微镜获得的结果。这项研究的结果有助于了解细胞中细胞凋亡诱导的最早机制,为药物测试和剂量反应分析提供了新方法。